Canonical Allele Identifier: CA2610045909
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI

Linked Data

gnomAD v4: 10-87863254-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863254C>T , CM000672.2:g.87863254C>T GRCh38
NC_000010.10:g.89623011C>T , CM000672.1:g.89623011C>T GRCh37
NC_000010.9:g.89612991C>T NCBI36
NG_007466.2:g.4817C>T , LRG_311:g.4817C>T
NG_033079.1:g.5184G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706954.1:c.-17+612C>T (PTEN) ENSP00000516674.1:n.-17+612C>T
ENST00000688308.1:c.-17+141C>T (PTEN) ENSP00000508752.1:n.-17+141C>T
ENST00000445946.5:c.-767G>A (KLLN) MANE Select ENSP00000392204.2:n.-767G>A
ENST00000371953.7:c.-1216C>T (PTEN) ENSP00000361021.3:n.-1216C>T
ENST00000445946.3:c.-767G>A (KLLN) ENSP00000392204.2:n.-767G>A
NM_001126049.1:c.-767G>A (KLLN) NP_001119521.1:n.-767G>A
NM_001126049.2:c.-767G>A (KLLN) MANE Select NP_001119521.1:n.-767G>A
Search 100 bp 5'
Search 100 bp 3'